Actively Recruiting

Age: 50Years +
MALE
NCT06852859

Patient-reported Pain and Symptom Relief During Three Months After Surgery for Benign Prostatic Hyperplasia

Led by Sahlgrenska University Hospital · Updated on 2025-05-16

500

Participants Needed

3

Research Sites

98 weeks

Total Duration

On this page

Sponsors

S

Sahlgrenska University Hospital

Lead Sponsor

V

Vastra Gotaland Region

Collaborating Sponsor

AI-Summary

What this Trial Is About

This is a prospective observational study in patients undergoing surgery for benign prostatic hyperplasia (BPH). The purpose of the study is to investigate in great detail patients' recovery after surgery for BPH regarding pain, hematuria, urine leakage and use of pain-relieving medications for three months postoperatively. Patient-reported outcomes after three different surgical methods will be investigated: transurethral resection, transurethral vaporization and laser transurethral enucleation of the prostate (Green-LEP) Research questions: * How do patients rate their day-to-day pain during the first three months after surgery for BPH? How long does it take to be pain free? * How does the patient estimate any day-to-day burning sensation during the first three months after surgery for BPH? * How many painkilling tablets of a certain preparation and a certain strength take patients per day in the first three months after surgery for BPH? * How long do patients have urinary leakage after surgery for BPH? * Are the patients bothered by possible urine leakage and if so for how long after surgery for BPH? * How long does one have macroscopic hematuria after surgery for BPH? * How quickly are the patients' urinary tract problems affected according to the IPSS per month? * Are the results on the above outcome measures different between the three TUR-P methods, TUV-P and Green LEP?

CONDITIONS

Official Title

Patient-reported Pain and Symptom Relief During Three Months After Surgery for Benign Prostatic Hyperplasia

Who Can Participate

Age: 50Years +
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing transurethral surgery for benign prostatic hyperplasia
  • Signed informed consent to participate
Not Eligible

You will not qualify if you...

  • Non-swedish speaking patients

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Alingsås lasarett, department of general surgery, urology and orthopaedic surgery

Alingsås, Sweden

Actively Recruiting

2

Kungälvs sjukhus, department of urology

Kungälv, Sweden

Not Yet Recruiting

3

NU sjukvården, Uddevalla sjukhus, department of urology

Uddevalla, Sweden

Not Yet Recruiting

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Research Team

J

Joakim BE Strömberg, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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